Medical Affairs Director

OverviewCook Medical is a leading manufacturer of medical devices, and we are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs department, you will play a crucial role in ensuring that our products meet the highest standards of quality and safety.ResponsibilitiesAssist in the running of Cook...

Job Description:The Senior Regulatory Scientist role is a critical position in the regulatory affairs team, responsible for assisting in the running of regulatory programmes and providing input into regulatory strategies.Key responsibilities include implementing regulatory requirements, maintaining an excellent understanding of global medical device...

We are looking for a talented Global Medical Device Strategist to join our team at Cook Medical. As a key member of our regulatory affairs department, you will be responsible for developing and implementing global regulatory strategies for our medical devices.Key ResponsibilitiesDevelop global regulatory strategies for Cook Medical devices in collaboration...

Job OverviewThe Regulatory Scientist 2 plays a vital role in developing regulatory strategies, ensuring compliance with global medical device regulations for specific jurisdictions.Maintains an excellent understanding of regulatory requirements in accordance with ISO13485, MDD 93/42/EEC, EU Medical Device Regulation 2017/745 and FDA QSP 21CFR Part...

Overview The Regulatory Affairs Specialist 2 ensures regulatory compliance to the EU MDR at the office of the EU Authorised representative (AR). The EU AR Office is responsible for verifying compliance to the EU MDR on behalf of Cook Medical's non-EU manufacturers. The Regulatory Affairs Specialist 2 serves as a communication liaison between the Cook...

Job DescriptionThe Senior Clinical Project Manager will collaborate with cross-functional teams, including Medical and Scientific Affairs, Clinical Affairs, and Global Clinical Affairs, to manage and complete studies in compliance with regulations like Good Clinical Practices (GCP), IVDR, and GDPR.Main Responsibilities:Leading and overseeing clinical...

Cook Medical is a leading manufacturer of medical devices, and we are seeking a highly skilled Compliance Officer for Medical Devices to join our team. As a key member of our regulatory affairs department, you will be responsible for ensuring that our products meet the highest standards of quality and safety.Key ResponsibilitiesAssist in the implementation...

Company Overview:Cook Medical is a leading manufacturer of medical devices, committed to improving patient outcomes through innovative products and services.Our company values innovation, quality, and customer satisfaction, and we strive to maintain the highest standards in our operations and regulatory compliance.We are seeking a highly skilled and...

Job Description:The Senior Clinical Project Manager will collaborate with the core team associates, extended core team associates, and Global Clinical Affairs associates, providing Medical and Scientific Affairs support within the various phases of product development and performance evaluation of the BD devices.Main Responsibilities:Represents Medical and...

Overview The primary function of this role is to provide leadership and direction to the Post Market and Manufacturing Engineering teams, while taking overall responsibility for effective and efficient running of the department. The Director, Engineering is also responsible for working with Local and Global Functional Leaders, and Divisions to manage all...

We are seeking a highly skilled Consultant Obstetrician & Gynaecologist to join our team at Red Chair Medical. This is a 12-month position offering a unique opportunity for a medical professional to provide high-quality patient care in Ireland.ResponsibilitiesHold full active IMC Specialist registration.Have recent experience in Obstetrics & Gynaecology,...

Consultant Obstetrician and GynaecologistWe are currently seeking a highly skilled Consultant Obstetrician & Gynaecologist to join our team at Red Chair Medical in Ireland. This is a 12-month position on a salary basis.Key ResponsibilitiesActive registration with the Irish Medical Council (IMC)Recent experience in obstetrics and gynaecology, preferably in a...

At Pale Blue Dot Recruitment, we are seeking an experienced Medical Device Industry Program Director to lead strategic initiatives within the medical device sector.In this role, you will manage cross-functional teams to deliver innovative healthcare solutions from concept through to regulatory approval and commercialization.The ideal candidate will bring...

We are the makers of possible BD is one of the largest global medical technology companies in the world.Advancing the world of health is our purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible...

Overview The primary role of the Senior Regulatory Scientist is to assist in the running of the regulatory affairs by providing input into: regulatory strategies, performing activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets and providing regulatory affairs input for the...

Job Description Summary The Senior Clinical Project Manager (Sr. CPM) will lead and oversee clinical performance evaluation studies for BD devices in Europe, focusing on the procurement of human bio-specimens for analytical and clinical studies. This role involves collaborating with cross-functional teams, including Medical and Scientific Affairs, Clinical...

Job Description Summary The Senior Clinical Project Manager (Sr. CPM) will lead and oversee clinical performance evaluation studies for BD devices in Europe, focusing on the procurement of human bio-specimens for analytical and clinical studies.This role involves collaborating with cross-functional teams, including Medical and Scientific Affairs, Clinical...

Overview The Regulatory Scientist 2 helps develop regulatory strategies, performs activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets. The Regulatory Scientist 2 serves as a communication liaison between the Cook manufacturer and the Cook local affiliates or regulatory...

Role OverviewThe Senior Clinical Project Manager will collaborate with the core team associates, extended core team associates, and Global Clinical Affairs associates to provide Medical and Scientific Affairs support within the various phases of product development and performance evaluation of the BD devices.This role requires a high level of expertise in...

Overview The Regulatory Scientist 2 helps develop regulatory strategies, performs activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets.The Regulatory Scientist 2 serves as a communication liaison between the Cook manufacturer and the Cook local affiliates or regulatory...